Cas 113572-93-3,2-Cyclopentene-1-carboxylic acid, 2-amino-1,3-bis[5-(benzoylamino)-1,3,4-thiadiazol-2-yl]-4,5-diphenyl-

113572-93-3

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Basic information

Product Name: 2-Cyclopentene-1-carboxylic acid, 2-amino-1,3-bis[5-(benzoylamino)-1,3,4-thiadiazol-2-yl]-4,5-diphenyl-
Synonyms:
CAS NO:113572-93-3
Molecular Formula: C36H27N7O4S2
Molecular Weight: 685.787
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Cyclopentene-1-carboxylic acid, 2-amino-1,3-bis[5-(benzoylamino)-1,3,4-thiadiazol-2-yl]-4,5-diphenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Cyclopentene-1-carboxylic acid, 2-amino-1,3-bis[5-(benzoylamino)-1,3,4-thiadiazol-2-yl]-4,5-diphenyl-(113572-93-3)
EPA Substance Registry System: 2-Cyclopentene-1-carboxylic acid, 2-amino-1,3-bis[5-(benzoylamino)-1,3,4-thiadiazol-2-yl]-4,5-diphenyl-(113572-93-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 113572-93-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113572-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,7 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113572-93:
(8*1)+(7*1)+(6*3)+(5*5)+(4*7)+(3*2)+(2*9)+(1*3)=113
113 % 10 = 3
So 113572-93-3 is a valid CAS Registry Number.

113572-93-3Upstream product

93355-74-9 N-(5-(1-cyano-2-phenylvinyl)-1,3,4-thiadiazol-2-yl)-benzamide

113572-93-3Downstream Products

113572-93-3Relevant academic research and scientific papers

Electroreduction of a Series of 2-Benzoylamino-5-(1-cyano-2-arylvinyl)-1,3,4-thiadiazoles

Fahmy, Hussein M.,Fattah, Nahed F. Abdel,Elmoghayar, Mohamed R. H.,Azzem, Magdy Abdel

, p. 1 - 6 (1988)

The electrochemical reduction of a series of 1,3,4-thiadiazoles in alcoholic buffered media has been investigated.The mechanism of the electrode processes is suggested and discussed.A cyclopentene carboxylic acid product is formed through a Ziegler-Throp reaction; the thiadiazole ring is inactive.Confirmation of the mechanism via c.p.e., spectrophotometric analyses, and the study of Hammett's relations is presented.

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